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Klaus Brusgaard

Showing results (21-30 of 94) with videos related to

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Frontiers in Endocrinology|June 28, 2021
CRISPR/Cas9 <i>ADCY7</i> Knockout Stimulates the Insulin Secretion Pathway Leading to Excessive Insulin SecretionYazeid Alhaidan, Henrik Thybo Christesen, Elena Lundberg, et al.
International Journal of Pediatric Otorhinolaryngology|April 2, 2018
Autosomal dominant stapes fixation, syndactyly, and symphalangism in a family with NOG mutation: Long term follow-up on surgical treatmentMarie Westergaard-Nielsen, Tine Amstrup, Jens Højberg Wanscher, et al.
European Journal of Medical Genetics|November 21, 2016
Boucher Neuhäuser Syndrome - A rare cause of inherited hypogonadotropic hypogonadism. A case of two adult siblings with two novel mutations in PNPLA6Jakob H Langdahl, Anja L Frederiksen, Nina Nguyen, et al.
Pediatrics|October 7, 2004
Laparoscopic diagnosis and cure of hyperinsulinism in two cases of focal adenomatous hyperplasia in infancyMonique De Vroede, N M A Bax, Klaus Brusgaard, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 27, 2007
Mosaic Turner syndrome and hyperinsulinaemic hypoglycaemiaHaya Alkhayyat, Henrik B T Christesen, James Steer, et al.
Current Problems in Cancer|July 15, 2020
Identification of genetic biomarkers in urine for early detection of prostate cancerEyyup Kavalci, Ali Ulvi Onder, Klaus Brusgaard, et al.
Skinmed|March 29, 2023
Identification of a Novel <i>PLCD1</i> Variant in a Danish Family with Hereditary LeukonychiaSofie Lieberoth, Sheetal Kumar, Klaus Brusgaard, et al.
Genetic Testing and Molecular Biomarkers|October 11, 2012
Allelic dropout in the ENG gene, affecting the results of genetic testing in hereditary hemorrhagic telangiectasiaPernille M Tørring, Anette D Kjeldsen, Lilian Bomme Ousager, et al.
Clinical Genetics|February 5, 2024
Identification of a founder variant AAGAB c.370C>T, p.Arg124Ter in patients with punctate palmoplantar keratoderma in Southern DenmarkStine Bjørn Gram, Anne Sofie Fredberg Jørgensen, Anette Bygum, et al.
Biochemical and Biophysical Research Communications|June 15, 2004
The primary defect in glycogen synthase activity is not based on increased glycogen synthase kinase-3alpha activity in diabetic myotubesMichael Gaster, Klaus Brusgaard, Aase Handberg, et al.
Pageof 10

Showing results (21-30 of 94) with videos related to

Sort By:
Pageof 10
Frontiers in Endocrinology|June 28, 2021
CRISPR/Cas9 <i>ADCY7</i> Knockout Stimulates the Insulin Secretion Pathway Leading to Excessive Insulin SecretionYazeid Alhaidan, Henrik Thybo Christesen, Elena Lundberg, et al.
International Journal of Pediatric Otorhinolaryngology|April 2, 2018
Autosomal dominant stapes fixation, syndactyly, and symphalangism in a family with NOG mutation: Long term follow-up on surgical treatmentMarie Westergaard-Nielsen, Tine Amstrup, Jens Højberg Wanscher, et al.
European Journal of Medical Genetics|November 21, 2016
Boucher Neuhäuser Syndrome - A rare cause of inherited hypogonadotropic hypogonadism. A case of two adult siblings with two novel mutations in PNPLA6Jakob H Langdahl, Anja L Frederiksen, Nina Nguyen, et al.
Pediatrics|October 7, 2004
Laparoscopic diagnosis and cure of hyperinsulinism in two cases of focal adenomatous hyperplasia in infancyMonique De Vroede, N M A Bax, Klaus Brusgaard, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 27, 2007
Mosaic Turner syndrome and hyperinsulinaemic hypoglycaemiaHaya Alkhayyat, Henrik B T Christesen, James Steer, et al.
Current Problems in Cancer|July 15, 2020
Identification of genetic biomarkers in urine for early detection of prostate cancerEyyup Kavalci, Ali Ulvi Onder, Klaus Brusgaard, et al.
Skinmed|March 29, 2023
Identification of a Novel <i>PLCD1</i> Variant in a Danish Family with Hereditary LeukonychiaSofie Lieberoth, Sheetal Kumar, Klaus Brusgaard, et al.
Genetic Testing and Molecular Biomarkers|October 11, 2012
Allelic dropout in the ENG gene, affecting the results of genetic testing in hereditary hemorrhagic telangiectasiaPernille M Tørring, Anette D Kjeldsen, Lilian Bomme Ousager, et al.
Clinical Genetics|February 5, 2024
Identification of a founder variant AAGAB c.370C>T, p.Arg124Ter in patients with punctate palmoplantar keratoderma in Southern DenmarkStine Bjørn Gram, Anne Sofie Fredberg Jørgensen, Anette Bygum, et al.
Biochemical and Biophysical Research Communications|June 15, 2004
The primary defect in glycogen synthase activity is not based on increased glycogen synthase kinase-3alpha activity in diabetic myotubesMichael Gaster, Klaus Brusgaard, Aase Handberg, et al.
Pageof 10